GINSENG WHITENING- niacinamide cream

Ginseng Whitening by

Drug Labeling and Warnings

Ginseng Whitening by is a Otc medication manufactured, distributed, or labeled by Synbio Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Niacinamide (2%)

Purpose

Skin Protectant/ brightening care

Uses

Helps to reduce the appearance of wrinkle, moisturize and brighten skin.

Keep out of reach of children

Do not swallow. In case of accidental ingestion, seek professional assistance.

Warnings

For external use only
Do not use when Your skin is red, inflamed, irritated or painful
When using this product
- Do not apply on other parts of the body
- Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
- Do not apply directly to wound or open cut.
Stop use and ask doctor if rash or irritation on skin develops and lasts.
Store at room temperature

Directions

Apply the adequate amount on skin anytime with a light pressing motion every day. Use more than twice a day.

Inactive Ingredients

D.I. Water, 1,3 Butylene Glycol, Cethylethyl Hexanoate, Glycerin, Caprylic/Capric Triglyceride, Glyceryl Oleate, Cetearyl Alcohol, Lecithin, Glyceryl Stearate, Tranexamic Acid, 1,2 Hexandiol, Ginsenoside, Glycerylstearate, PEG-100 Stearate, Polyglyceryl -3, Methylglucos Distearate, Citrus Paradisi (Grapefruit) Fruit Extract, Sodium Hyaluronate, Dimethicone, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Arnica Montana Flower Extract, Portulaca Oleracea Extract, Camellia Sinensis Leaf Extract, Poloxamer 407, Polysorbate 80, Isohexadecane, Phenoxyethanol, Citric Acid, Perfume

Ginseng Whitening Cream

INGREDIENTS AND APPEARANCE

GINSENG WHITENING 
niacinamide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70969-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	Niacinamide	2 g  in 50 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
Glycerin (UNII: PDC6A3C0OX)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
Glyceryl Oleate (UNII: 4PC054V79P)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
TRANEXAMIC ACID (UNII: 6T84R30KC1)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
GINSENOSIDES (UNII: 3K198YD54P)
PEG-100 STEARATE (UNII: YD01N1999R)
POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
GRAPEFRUIT (UNII: O82C39RR8C)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
Dimethicone (UNII: 92RU3N3Y1O)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
PURSLANE (UNII: M6S840WXG5)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
POLOXAMER 407 (UNII: TUF2IVW3M2)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
ISOHEXADECANE (UNII: 918X1OUF1E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70969-101-02	1 in 1 PACKAGE	09/19/2016
1	NDC: 70969-101-01	50 g in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/19/2016

Labeler - Synbio Co., Ltd. (557821393)

Registrant - Synbio Co., Ltd. (557821393)

Establishment
Name	Address	ID/FEI	Business Operations
Synbio Co., Ltd.		557821393	manufacture(70969-101)